CRISPR and Gene Editing

CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) technology has revolutionized gene editing, offering precise and efficient ways to modify DNA. In stem cell research, it enables targeted genetic corrections, disease modeling, and the development of personalized therapies. By leveraging CRISPR, researchers are advancing regenerative medicine, genetic disease treatment, and creating improved stem cell models for drug discovery. The potential for CRISPR in stem cell therapies is immense, driving innovations in personalized medicine and transformative healthcare solutions

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